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Page 196 of 547-
Neurogenesis and neuron regeneration in the olfactory system of mammals. III. Deafferentation and reinnervation of the olfactory bulb following section of the fila olfactoria in rat.
Axotomy at the level of the lamina cribrosa in rat induces rapid degeneration of the olfactory sensory axons in the bulb. The phenomenon, which is limited to the layer of olfactory fibres and to the glomeruli of the bulb, can be observed as early as 15-24 h after surgery, and peaks at 3-4 days. The glomeruli located in the rostro-ventral portion of the bulb are affected first, and the process extends to the dorso-caudal portion with a delay of 12-24 h. Reactive hypertrophy of the glia coincides with removal of the degenerating terminals, and is maximal 48 h after axotomy. Axotomy does not preclude reinnervation of the bulb by axons originating from new, reconstituted neurons in the olfactory neuroepithelium. These new axons begin to reach the periphery of the bulk approximately at the 20th day post-operative and then reinnervate the glomeruli. The rostro-ventral portion of the bulb is the first to be reinvaded by the new axons. The glomeruli reacquire a morphological pattern similar to controls between 20 to 30 days.
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On the occurrence of a myeloid body in pinealocytes of the white-footed mouse, Peromyscus leucopus. An electron-microscopic study.
The fine-structural features of pinealocytes of the white-footed mouse, Peromyscus leucopus, were examined. A single population of pinealocytes was observed in both superficial and deep components of the gland. Cells in both locations are characterized by the presence of an indented nucleus exhibiting a prominent nucleolus. The usual organelles in the perikaryon are the Golgi complexes, mitochondria, endoplasmic reticulum, polysomes, microtubules and dense-core vesicles. In addition the perikaryonal cytoplasm often contains a single myeloid body. These bodies are usually lenticular in shape, are formed of an array of flattened membranous cisternae, and are not bounded by a limiting membrane. This organelle usually lies in the vicinity of the nucleus and is infrequently associated with lipid bodies. Complex forms were also observed. The cisternae are continuous with elements of the endoplasmic reticulum at points along their expanded rims. The outer surface of the cisternal membrane exhibits a granularity or fuzziness. The cisternae may be fenestrated. Pinealocyte processes with an abundance of clear vesicles, and some dense-core vesicles and vesicle-crowned rodlets are present in the parenchyma.
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Intracellular dynamics in pituitary mammotropes throughout the rat estrous cycle. II. Changes in synthetic and secretory organelles.
The organellar dynamics within mammotropes (prolactin secreting cells) of the anterior pituitary were examined using morphometry throughout the four-day rat estrous cycle. Two predominant periods of maximal organellar activity were found. The first period, which occurred during proestrus, resulted in two peaks of serum PRL at 6 pm and 12 m proestrus, while the second occurred during middiestrus-2 and resulted in an increase of pituitary PRL, but not a major serum PRL peak. The mitochondrial volume rose prior to that of other organelles during early proestrus, rising 110% from 4 am late diestrus-2 to 6 pm proestrus. However, the number of mitochondria per cell remained constant throughout the cycle. The volumes of rough endoplasmic reticulum (RER) and Golgi complex reached maximal proportions at 8 pm and 12 m proestrus, respectively. The RER volume was 153% greater than at 4 am late diestrus-2, while the Golgi complex had increased by 200%. We suggest that changes in the RER and Golgi complex volumes were the result of two processes: the synthesis of new membrane and the swelling of existing complexes. This study further substantiated that the serum peak of PRL at 6 pm proestrus is the result of stored mature granules being released, whereas the PRL peak at 12 m proestrus is due to the immediate release of hormone without any storage.
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Ultrastructure of the subfornical organ of the chicken (Gallus domesticus).
The SFO of the chicken is divided in half by a large central blood sinus; ventrally it is covered by a thin layer of ependyma (including tanycytes, dendrites, and axons) which connects the two lateral halves and protrudes as a midsagittal crest into the lumen of the third ventricle. The ependyma consists predominantly of tanycytes with long basal processes which terminate upon perivascular spaces. These cells have an extensive Golgi apparatus and abundant lysosomes; their cellular apices containing polyribosomes and a few vesicles frequently protrude into the ventricle. In addition to astrocytes, oligodendrocytes, and microglial cells, there is another glial cell population that is distinguished by the presence of parallel stacks or spherical to ovoid conglomerates of rough ER and their unique location, i.e., limited to areas ventral and ventral-lateral to the large blood sinus. Two types of neurons are present: neurons in which there is a paucity of granulated vesicles and occasional vacuoles in both the cytoplasm and nuclei, the second type of neuron elaborates many granulated vesicles. Numerous puncta adhaerentia are observed between adjacent neuronal perikarya and between glial processes and neuronal perikarya. Diverse axon types are found within the chicken SFO. Axo-dendritic and axo-somatic axon terminals and presynaptic axon dilations contain assorted combinations of electron-lucent and granulated vesicles of different maximal diameters. Based on the morphology of these axons, cholinergic, peptidergic, and serotoninergic fibers are described. There are two additional groups of axons whose classification awaits further investigation. The chicken SFO differs from the mammalian SFO in several respects: it possesses an ependyma with secretory and/or absorptive tanycytes predominating; it is divided midsagittally by a central blood sinus; its lateral and dorsal limits are nebulous; a previously undescribed peculiar type of glial cell is found in a limited portion of the organ; supraependymal neurons are lacking.
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Pyridoxal phosphatase: cytochemical localization in GERL and other organelles of rat neurons.
A phosphatase, hydrolyzing pyridoxal-5-phosphate (P5P), a physiologically active component of the vitamin B6 complex and an essential co-enzyme in the synthesis of neurotransmitters, has been localized cytochemically in the perikarya of neurons in the peripheral, autonomic and central nervous systems of the rat. Neurons in dorsal root ganglia, sympathetic ganglia and ventral horn of spinal cord were studied by light and electron microscopy, while Purkinje cells, neurons in the dentate nucleus of the cerebellum, thalamus, and hypothalamus were studied by light microscopy only. Optimal conditions for demonstrating this activity in aldehyde-fixed tissue were determined with dorsal root ganglia. At the optimal pH of 5.0, neurons in these ganglia and in all other neurons studied show pyridoxal-5-phosphatase (P5Pase) activity in GERL. Small neurons in dorsal root ganglia also display enzyme activity in the endoplasmic reticulum (ER); activities in GERL and ER are also appreciably high at neutral pH. Small and large neurons in these ganglia, and neurons of sympathetic ganglia, show variable P5Pase activity in the Golgi apparatus. These localizations differ from the usual sites of both acid phosphatase and alkaline phosphatase activities. The P5Pase activity, demonstrated cytochemically, is a new acid hydrolase activity in GERL.
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Phagocytic activity of the stellate cells in the anuran pars intermedia.
In an attempt to study further the stellate cell and its functions, the ultrastructure of this cell type in the neurointermediate lobe of the bullfrog, Rana catesbeiana, was examined in both organ and dissociated-cell culture. The cytoplasmic activity of stellate cells from neurointermediate lobes incubated 3 1/2 or 5 1/2 h was greater than that of those in vivo. Mitochondria and bundles of cytoplasmic filaments were numerous, in addition to prominent, well-developed Golgi complexes with associated vesicles. The most striking ultrastructural feature was the presence of phagocytic vacuoles that contain cellular debris. The stellate cells were seen to form cytoplasmic processes that phagocytosed this extracellular debris identifiable as belonging to the secretory cells of the pars intermedia. The stellate cells from the dissociated-cell preparations were also seen to contain debris within phagocytic vacuoles. In those neurointermediate lobes transplanted for 3 1/2 to 4 days into the anterior chamber of the eye, the stellate cells demonstrated similar phagocytic ability, but the phagocytic vacuoles contained material that seemed to be at a later stage of degradation. In all three of these conditions, the stellate cells were not seen to release this cellular debris nor were they seen to undergo cell division. These glial-like stellate cells of the pars intermedia acted as macrophages in all three of these experiments. There is now, therefore, a need to determine under what conditions, if any, these stellate cells function in vivo as macrophages.
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Axonal transport of proteins in the hypothalamo-neurohypophysial system of the rat.
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Ultrastructure of the pineal gland of the brush mouse (Peromyscus boylei): influence of long and short photoperiod.
The ultrastructure of the pineal gland of wild-captured brush mice (Peromyscus boylei) was examined. A homogeneous population of pinealocytes was present in the pineal gland of this species. The Golgi apparatus, granular endoplasmic reticulum, mitochondria, lysosomes, dense-core vesicles, vacuoles containing fluocculent material, clear vesicles, microtubules and glycogen particles were consistent components of the pinealocyte cytoplasm; infrequently-observed organelles included centrioles, "synaptic" ribbons, subsurface cisternae, multivesicular bodies, lipid droplets and annulate lamellae-like structures. Quantitative comparison of pinealocyte ultrastructure revealed larger cross-sectional areas of cytoplasma, nucleus, Golgi apparatus, granular endoplasmic reticulum, mitochondria and vacuoles containing flocculent material as well as higher number of dense-core vesicles in the animals kept in short photoperiod (LD 8 : 16) as compared to those in animals kept in long photoperiod (LD 16 : 8). These observations suggest that restricting the amount of light to which animals are exposed activated the pinealocytes of brush mice.
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Morphologic development of neonatal rat pinealocytes in monolayer culture.
The morphological development of pinealocytes maintained in monolayer culture, without the neural and humoral effects present in the developing rat has been studied and compared with the development that occurs in vivo. Pinealocytes in 5 day cultures contained organelles that were similar to those present in the pineals of intact 5 day old rats. However, light and dark cells were not noted in culture, and the cultured cells did not have the dense granules noted in vivo. As pinealocytes developed in culture, cytoplasmic processes increased in length and number. By 21 days of culture age, synaptic ribbons were found to have decreased in number, the difference between light cell and dark cell cytoplasm had become more prominent, and dense-cored vesicles had become more numerous, just as in the developing gland in vivo. These results suggest that the complex neural and humoral factors impinging upon the developing neonatal pineal in the intact animal may not be necessary for some aspects of its ultrastructural differentiation.
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Interactions between tectal radial cells in the red-eared turtle, Pseudemys scripta elegans: an analysis of tectal modules.
The optic tectum is a major subdivision of the visual system in reptiles. Previous studies have characterized the laminar pattern, the neuronal populations, and the afferent and efferent connections of the optic tectum in a variety of reptiles. However, little is known about the interactions that occur between neurons within the tectum. This study describes two kinds of interactions that occur between one major class of neurons, the radial cells, in the optic tectum of Pseudemys using Nissl, Golgi and electron microscopic preparations. Radial cells have somata which bear long, radially oriented apical dendrites from their upper poles and short, basal dendrites from their lower poles. They are divided into two populations on the basis of the distribution of their somata in the tectum. Deep radial cells have somata densely packed in the stratum griseum periventriculare. Their plasma membranes form casual appositions. Middle radial cells have somata scattered throughout the stratum griseum centrale and stratum fibrosum et griseum superficiale and do not contact each other. The apical dendrites of both populations of radial cells participate in vertically oriented, dendritic bundles. The plasma membranes of the dendrites in these bundles form casual appositions in the deeper tectal layers and chemical, dendrodenritic synapses within the stratum fibrosum et griseum superficiale. The synapses have clear, round synaptic vesicles and slightly asymmetric membrane densities. Thus, radial cells interact via both casual appositions and chemical synapses. These interactions suggest that radial cells may form a basic framework in the tectum. Because both populations of radial cells extend into the stratum fibrosum et griseum superficiale and stratum opticum, they may receive input from some of the same tectal afferent systems. Because the deep radial cells alone have somata and dendrites in the deep tectal layers, they may receive additional inputs that the middle radial cells do not. Neurons in the two populations interact via chemical dendrodentritic synapses, thereby forming vertically oriented modules in the tectum.